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Micropatterned Surfaces to Study Hyaluronic Acid Interactions with Cancer Cells
Published on: December 22, 2010
Hyaluronic Acid-Based Nanomaterials Applied to Cancer: Where Are We Now?
Vera Machado1, Mariana Morais1,2, Rui Medeiros1,2,3,4,5
1Molecular Oncology and Viral Pathology Group, Research Center of IPO Porto (CI-IPOP)/RISE@CI-IPOP (Health Research Network), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center (Porto.CCC), Research Center-LAB2, E Bdg 1st Floor, Rua Dr António Bernardino de Almeida, 4200-072 Porto, Portugal.
Abstract:
Cancer cells normally develop the ability to rewire or reprogram themselves to become resistant to treatments that were previously effective. Despite progress in understanding drug resistance, knowledge gaps remain regarding the underlying biological causes of drug resistance and the design of cancer treatments to overcome it. So, resistance acquisition remains a major problem in cancer treatment. Targeted therapeutics are considered the next generation of cancer therapy because they overcome many limitations of traditional treatments. Numerous tumor cells overexpress several receptors that have a high binding affinity for hyaluronic acid (HA), while they are poorly expressed in normal body cells. HA and its derivatives have the advantage of being biocompatible and biodegradable and may be conjugated with a variety of drugs and drug carriers for developing various formulations as anticancer therapies such as micelles, nanogels, and inorganic nanoparticles. Due to their stability in blood circulation and predictable delivery patterns, enhanced tumor-selective drug accumulation, and decreased toxicity to normal tissues, tumor-targeting nanomaterial-based drug delivery systems have been shown to represent an efficacious approach for the treatment of cancer. In this review, we aim to provide an overview of some in vitro and in vivo studies related to the potential of HA as a ligand to develop targeted nanovehicles for future biomedical applications in cancer treatment.
Insights
Cancer cells develop resistance to treatments. Hyaluronic acid (HA) targets cancer cells, offering a promising strategy for developing advanced nanomedicines to overcome drug resistance and improve cancer therapy.
Area of Science:
- Biomedical Engineering
- Oncology
- Materials Science
Background:
- Cancer cells acquire resistance to conventional therapies, necessitating novel treatment strategies.
- Targeted therapeutics offer advantages over traditional treatments by overcoming limitations.
- Tumor cells often overexpress receptors for hyaluronic acid (HA), which are less common in normal cells.
Purpose of the Study:
- To review the potential of hyaluronic acid (HA) as a targeting ligand for nanovehicles in cancer treatment.
- To explore in vitro and in vivo studies demonstrating HA's role in targeted drug delivery.
- To highlight HA-based nanocarriers for future biomedical applications in oncology.
Main Methods:
- Review of in vitro and in vivo studies on HA-targeted nanovehicles.
- Analysis of HA's properties for drug conjugation and formulation (e.g., micelles, nanogels, nanoparticles).
- Evaluation of HA-based drug delivery systems for tumor-selective accumulation and reduced toxicity.
Main Results:
- Hyaluronic acid (HA) exhibits biocompatibility and biodegradability, suitable for drug conjugation.
- HA-based nanocarriers demonstrate enhanced tumor-selective drug accumulation and predictable delivery.
- These systems show potential for decreased toxicity to normal tissues compared to conventional treatments.
Conclusions:
- Hyaluronic acid (HA) is a promising ligand for developing targeted nanovehicles in cancer therapy.
- HA-based nanomaterial drug delivery systems offer an effective approach to overcome cancer drug resistance.
- Further research into HA-targeted nanomedicines holds significant potential for future cancer treatment applications.
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